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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 528896Erstellt: 23. Oktober 2026

Butanal → N-butyl-4-(4-fluorophenoxy)aniline

https://huagongshe.com/de/reaction/528896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanalHCID 261—
EduktBenzenamine, 4-(4-fluorophenoxy)-HCID 147633—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktN-butyl-4-(4-fluorophenoxy)anilineHCID 7108630262,7%

Reaktionsschritte

To a solution of 4-(4-fluorophenoxy)aniline (Apollo, 500 mg, 2.46 mmol) and butyraldehyde (240 μL, 2.71 mmol) in DCE (5.0 mL) were added 4 Å molecular sieves. The resulting reaction mixture was stirred at room temperature for 1 h. Next, Na(OAc)3BH (782 mg, 3.69 mmol) was added, and the reaction mixture was stirred at room temperature overnight. Concentration in vacuo afforded a crude residue which was purified by flash column chromatography (10% EtOAc/hexanes) to give the title compound (400 mg, 62%). 1H NMR (CDCl3) δ 7.28-7.21 (m, 2H), 7.20-7.13 (m, 4H), 6.91-6.85 (m, 2H), 3.82 (br s, 1H), 3.39 (t, J=7.0 Hz, 2H), 1.96-1.85 (m, 2H), 1.79-1.67 (m, 2H), 1.26 (t, J=7.4 Hz, 3H); MS(ESI+) m/z 260.1 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09346795B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-e402595823f047f3ab20ee2c6fba20af
Quellennotizuspto-grants-2016_05